Scoliosis correction systems, methods, and instruments

ABSTRACT

Devices, systems and methods for use in spinal surgeries. The system may include a fastener system comprising a fastener, a staple, and a locking cap. A cord may extend along the spine and through at least one fastener system. An instrument may be provided for tensioning the cord. The system may, for example, apply fixation on the convexity of the scoliotic vertebrae to limit growth on the convex side and allow unilateral growth on the concave side.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to U.S. Provisional Application No.62/636,212, filed Feb. 28, 2018, which is incorporated by referenceherein in its entirety for all purposes.

FIELD

The present disclosure provides devices, systems, and instruments foruse in spinal surgeries.

BACKGROUND

The vertebrate spine is the axis of the skeleton providing structuralsupport for the other parts of the body. Scoliosis is a term used todescribe any abnormal, sideway curvature of the spine. The most commonform of scoliosis for patients between the age of 10 and 18 years istermed adolescent idiopathic scoliosis (AIS). Although the particularcause of this type of scoliosis is still unknown, advancements in themedical field have enabled doctors to increase the likelihood ofsuccessfully treating scoliosis.

One type of spinal surgery for treating scoliosis is the use ofimplantable rods. One or more rods are implanted into the patientthrough the back of the spine. The rods may be secured to the spine tocorrect the condition. There remains a need for improved systems thatfacilitate scoliosis correction and serve as a means for deformitycorrection with or without fusion.

SUMMARY

To meet this and other needs, scoliosis correction devices, systems,methods, and instruments are provided. The systems offer implants andinstruments for deformity correction with or without fusion. Traditionalrods or a flexible, durable, biocompatible cord may be secured to thespine. The system may apply fixation on the convexity of the scolioticvertebrae to limit growth on the convex side and allow unilateral growthon the concave side. The system creates an optimized construct forspinal alignment to maintain stability while allowing growth inskeletally immature patients. In addition, the instruments facilitaterod or cord insertion and/or tensioning, for example, using an anterioror posterior approach.

According to one embodiment, a spinal system includes a fastener systemcomprising a fastener, a staple, and a locking cap. The fastener has athreaded portion and a head portion configured to move relative to thethreaded portion. The staple includes a ring configured to surround thethreaded portion of the fastener and a plurality of prongs configured toengage bone. A rod or cord may be provided in the system and isconfigured to be retained within one or more of the fastener systems.The rod or cord may be tensioned to impart a compressive force to thescoliotic vertebrae.

According to another embodiment, a spinal system includes a firstfastener system, a second fastener system, and a cord. The firstfastener system includes a first fastener, a first staple, and a firstlocking cap. The first fastener has a first threaded portion and a firsthead portion configured to move relative to the first threaded portion.The first staple includes a first ring configured to surround the firstthreaded portion of the first fastener and a first plurality of prongsconfigured to engage bone. The second fastener system includes a secondfastener, a second staple, and a second locking cap. The second fastenerhas a second threaded portion and a second head portion configured tomove relative to the second threaded portion. The second staple includesa second ring configured to surround the second threaded portion of thesecond fastener and a second plurality of prongs configured to engagebone. The cord extends between at least the first fastener system andthe second fastener system. The cord is tensioned between the firstfastener system and the second fastener system, for example, to correcta curve of the spine.

According to another embodiment, an instrument for tensioning the cordincludes a body having an opening. The opening receives a compressortube, and the compressor tube receives a threaded shaft therethrough.The cord is configured to be affixed to a distal end of the threadedshaft. Movement of the threaded shaft applies a compressive force to thecord to tension the cord within the fastener system.

According to yet another embodiment, an instrument for tensioning thecord may include a first portion and a second portion coupled to thefirst portion at a pivot point, thereby pivotally connecting the firstand second portions together. The first portion includes a first tubularmember and the second portion includes a second tubular member. Thefirst and second tubular members are aligned along a common axis suchthat the opening is a central longitudinal opening extending through thefirst and second tubular members. In a second position, the first andsecond tubular members are not aligned along the common axis and areangled relative to one another. The first portion includes a firsthandle portion extending from the first tubular member and the secondportion includes a second handle portion extending from the secondtubular member. Distal ends of the first and second handle portions maybe connected with a ratchet. The ratchet may extend from the distal endof the second handle portion at a pivot, and the ratchet is engagablewith a pawl on the first handle portion. The ratchet may include aplurality of uni-directional teeth. The instrument may include a forcegauge and a plurality of indicia, and when the force gauge moves, theplurality of indicia indicate the amount of compressive force on thecord and provided by the instrument.

According to yet another embodiment, an instrument for tensioning thecord includes a first, main handle that grasps the compressor tube andthe threaded shaft. The instrument may include a second handle (e.g., aT-handle) or a knob. When using two handles, the two handles may bepulled apart from one another to impart the compressive forces on thecord. As an alternative to the T-handle, a knob may be used. The knobmay have an internal thread to threadedly engage the threaded shaft. Theknob may be turned to apply the compressive force to the cord.

According to yet another embodiment, a method of installing the systemmay include inserting one or more staples into an anterior aspect ofeach vertebral body. After the staple is fully seated against thevertebral body, the fastener may be inserted through the opening in thestaple. Once the fasteners are placed, the cord may be selected andpositioned within the heads of each fastener. The non-threaded lockingcaps may be installed in the heads of the fasteners. The cord istensioned, for example, with the one or more instruments describedherein, and after final tensioning of the cord, the locking caps arefully tightened to maintain the tension on the cord.

According to yet another embodiment, a kit includes one or more of thecomponents, implants, instruments, or systems described herein. Forexample, the kit may include a plurality of fastener systems, forexample, of different sizes, cords and/or rods, and one or moreinstruments including instruments for inserting and/or tensioning thecord.

BRIEF DESCRIPTION OF THE DRAWINGS

A more complete understanding of the present disclosure, and theattendant advantages and features thereof, will be more readilyunderstood by reference to the following detailed description whenconsidered in conjunction with the accompanying drawings wherein:

FIG. 1 is a perspective view of a spine with a spinal system accordingto one embodiment;

FIG. 2 is a perspective, exploded view of a fastener system for use withthe spinal system of FIG. 1;

FIG. 3 is an exploded view of instrument for use with inserting and/ortensioning a cord within the spinal system of FIG. 1;

FIG. 4 is a close-up view of the cord attached to the threaded rod ofthe instrument in FIG. 3;

FIG. 5 is an assembled view of the instrument of FIG. 3;

FIG. 6 is a perspective view of the instrument of FIG. 3 with thecompressor tube and shaft removed for clarity;

FIG. 7 is a compressed view of the instrument of FIG. 6 to tension thecord within the spinal system of FIG. 1;

FIG. 8 is an alternative version of an instrument suitable fortensioning the cord according to another embodiment;

FIG. 9 is another version of an instrument suitable for tensioning thecord according to another embodiment; and

FIGS. 10-16 depict additional systems for tensioning the cord accordingother embodiments.

DETAILED DESCRIPTION

Embodiments of the disclosure are generally directed to scoliosiscorrection devices, systems, methods of use, and instruments forinstalling the same. The scoliosis correction system may be used toapply fixation on the convexity of the scoliotic vertebrae. A rod orflexible cord, for example, may be used to limit growth on the convexside and allow unilateral growth on the concave side of the spine.

Referring now to FIG. 1, a scoliosis correction system 100 may includeone or more fastener systems 110 secured to bone or vertebrae 10. Thefastener systems 110 may be attached to an anterior aspect of each ofthe vertebral bodies 10, for example, adjacent to the rib head. Althoughseven fastener systems 110 are exemplified in the system 100 shown inFIG. 1, it will be appreciated that the surgeon could select anysuitable number of fastener systems 110 as the surgeon deems appropriateto correct the deformity. The one or more fastener systems 110 areconfigured to retain a traditional rod or a cord 140 extending from afirst end 142 to a second end 144. The rod or cord 140 is configured tobe retained within the fastener systems 110 and tensioned tointraoperatively correct the deformity of the spine. The scoliosiscorrection system 100 may be implanted using an anterior or posteriorspinal approach, for example. In particular, the system 100 may beimplanted through a thoracoscopic approach or a mini-open thoractotomyto help minimize tissue disruption and/or scar tissue formation. Thetensioned rod or cord 140 may provide for spinal alignment to maintainstability while allowing growth in skeletally immature patients.

The cord 140 may be a cable, wire, band, flexible or elastic member, forexample. In one embodiment, the cord 140 is a narrow, flexible band. Insome embodiments, the cord 140 is between 250-800 mm in length, forexample, or may be cut to length, but any suitable length may beselected based on the deformity being corrected. As shown, the cord 140is a single continuous cord extending from the first end 142 to thesecond 144, but it is also envisioned that more than one cord may beused or a section thereof may be coupled to another cord, rod, or otherdevice, if desired. In some embodiments, the cord 140 is composed of apolymer, such as polyethylene terephthalate (PET), but any suitablebiocompatible material may be selected. Preferably, the cord 140 is ableto be placed under tension to achieve the proper amount of correction tothe spine without fusion.

Turning to FIG. 2, the fastener system 110 may include a fastener 112, astaple 120, and a locking cap 130. The fastener 112 may extend from adistal end 102 to a proximal end 104. The distal end 102 may beconfigured to be received with the bone 10, and the proximal end 104 maybe configured to sit above the bone 10. The fastener 112 may include ashaft portion or a threaded portion 114 and a yoke, tulip, or headportion 116. The threaded portion 114 may terminate at the distal end102, for example, as a point, tapered to a narrowed end, or a blunt tipto facilitate insertion in the bone 10. In one embodiment, the distalend 102 may form a blunt tip for safe bicortical purchase in the bone10. The threaded portion 114 may include any suitable type of threading.In one embodiment, the thread includes a double lead thread for rapidinsertion, for example.

The yoke, tulip, or head portion 116 may be configured to move relativeto the threaded portion 114. In one embodiment, the head portion 116 maybe able to pivot about a longitudinal axis defined by the shaft portionof the fastener 112, thereby allowing for monoaxial movement of the headportion 116 relative to the threaded portion 114. In another embodiment,the head portion 116 may be able to move in a polyaxial manner relativeto the threaded portion 114. It is also envisioned that the head portion116 may be fixed relative to the threaded portion 114.

The head portion 116 of the fastener 112 may be in the form of a yoke ortulip defining a bore 106 therethrough, a body 108, and arms 118 thatextend upwardly from the body 108. As shown in FIG. 2, the arms 118 maydefine a U-shaped channel sized to receive rod or cord 140. Each of thearms 118 has an interior surface configured to engage with the lockingcap 130. Each of the arms 118 may also include an outer surface whichdefines a tool engagement groove for holding the head portion 116 with asuitable tool (not illustrated).

The locking cap 130 may be formed of two parts: an outer portion 132 andan inner portion 134. The outer portion 132 may define an openingtherethrough for receiving the inner portion 132. The outer portion 132may provide a non-threaded interface with the head portion 116 of thefastener 112. The inner portion 132 may be threaded to engage withinterior threads within the outer portion 132. One or more features ofthe head portion 116 and locking cap 130 may be similar to thosedescribed in U.S. Pat. No. 8,888,827, which is incorporated by referenceherein in its entirety for all purposes.

The fastener system 110 may further include a staple 120. The staple 120may be formed of a ring 122 defining an opening 126. The ring 122 may beconfigured to surround the threaded portion 114 of the fastener 112 anda plurality of prongs 124 may extend from the ring 122 and areconfigured to engage the bone 10. In the embodiment shown, the ring 122is a continuous ring, but it may also be split or otherwise shaped. Inaddition, the embodiment shown provides for three prongs 124 extendingdownwardly from the ring 122 and toward the distal end 102 of thefastener 112. The prongs 124 may help to increase the vertebral bodyfixation and/or increase resistance to screw toggle. Although threeprongs 124 are exemplified, it will be appreciated that a differentnumber or orientation of the prongs 124 may be selected.

The system 100 or components thereof may be comprised of any suitablebiocompatible materials. For example, the staples 120, fasteners 112,and locking caps 130 may be manufactured from various biocompatiblematerials, such as metals, polymers, ceramics or combinations thereof.Exemplary materials include titanium (and titanium alloys),cobalt-chrome, stainless steel, and/or polyetheretherketone (PEEK), forexample. In one embodiment, the fastener 112 (e.g., the threaded portion114) is coated with a hydroxyapatite (HA) coating, which may help topromote bony ongrowth.

When installing the system 100, the one or more staples 120 may beinserted first or in tandem with the fastener 112. In one embodiment,the staples 120 may be positioned on the anterior aspect of thevertebral body 10. After the staple 120 is fully seated with a bottomsurface of the ring 122 against an outer surface of the bone 10, thefastener 112 may be inserted through the opening 126 in the ring 122.The fastener 112 may be driven into the vertebral body 10 through thecenter of the staple 120. This process is repeated for all desiredlevels. Once the fastener systems 110 are placed, the cord 140 may beselected and cut to length. The cord 140 is positioned within the headportions 116 of each fastener 112. After the cord 140 is positionedwithin the head portion 116 of the fastener 112, the locking cap 130 maybe positioned within the opening 106 such that the outer portion 132 isnon-threadedly locked to the head portion 116 (e.g., rotated 90degrees). This allows the cord 140 to be captured within the headportion 116 but still able to be tensioned. After final tensioning ofthe cord 140 is achieved, the inner portion 134 of the locking cap 130may be rotated and threaded downwardly to contact and secure the cord140 in its final position.

Turning now to FIGS. 3-6, an instrument 200 for tensioning a cord, forexample, the cord 140 in system 100, according to one embodiment will bedescribed. The instrument 200 may be configured to compress the spineduring a thoracoscopic or open anterior spinal deformity correctionprocedure, for example. The instrument 200 may work with either a fusionor non-fusion procedure. It may be ineffective to compress the spine bymanipulating minimally invasive surgical (MIS) tubes outside the woundbecause the tubes tend to flex. Instead, instrument 200 may be used inorder to compress at the level of the respective fasteners 112.Furthermore, the instrument 200 is able to fit within a round, tubularport (e.g., 15 mm diameter) which is placed in the space betweenadjacent ribs. The instrument 200 can exert a suitable amount ofcompression on the spine, for example, approximately up to 440N [100lbf] maximum.

The instrument 200 may include a first portion 202 and a second portion204 coupled to the first portion 202 at a pivot point 206. The pivotpoint 206 may be provided by a pivot pin or other suitable mechanism toallow for pivotally connecting the first and second portions 202, 204together. The first portion 202 includes a first tubular member 208 andthe second portion 204 include a second tubular member 210. In a firstposition (e.g., shown in FIG. 3), the first and second tubular members208, 210 are aligned along a common axis such that a centrallongitudinal opening extends therethrough. The first portion 202 definesa first handle portion 212 extending from the first tubular member 208and the second portion 204 defines a second handle portion 214 extendingfrom the second tubular member 210. In a second, compressed position(e.g., shown in FIG. 7), the first and second tubular members 208, 210are not aligned along a common axis and are angled relative to oneanother.

The distal ends of the first and second handle portions 212, 214 may beconnected with a ratchet 216. The ratchet may extend from the distal endof the second handle portion 214, for example, at a pivot 220, andengage with a pawl 222 on the first handle portion 212. When the firstand second handle portions 212, 214 are squeezed towards one another,the pawl 222 can translate along teeth 218 on an upper surface of theratchet 216 to maintain the first and second handle portions 212, 214 inthe compressed configuration (e.g., shown in FIG. 7). The teeth 218 maybe uni-directionally oriented to allow movement of the first handle 212towards the second handle 214. The ratchet 216 may be disengaged fromthe pawl 222 to release the first handle portion 212 relative to thesecond handle portion 214. One or more springs 224 may be provided alonginner surfaces of the handle portions 212, 214 to provide resistance tothe instrument 200.

The first tubular member 208 may define a gauge sleeve 227 and aplurality of indicia 226. When the force gauge 227 moves, the pluralityof indicia 226 may indicate the amount of compression force provided bythe instrument 200. For example, the plurality of indicia 226 may beetchings provided, for example, in 100N increments. The second tubularmember 208 may retain a button 228 configured to unlock the shaft 234and allow the cord 140 to move within the instrument 200.

In operation, a sleeve or compressor tube 230 is inserted into opening225 in the first tubular member 208. A cap 232 may be place on the endof the compressor tube 230 opposite the end that was inserted into theinstrument 200. The cap 232 may be, for example, a PEEK cap that isfirmly secured to the end of the compressor tube 230. Next, a shaft 234may be inserted into the open end of the tube 230. The shaft 234 may bea threaded shaft 234 that is threaded along a portion or the entirelength of the shaft 234. The shaft 234 may be a flexible threaded rod,for example, constructed of polyetheretherketone (PEEK),polyoxymethylene (POM), or a similar flexible plastic. The threadedshaft 234 may have a chuck or collet 236 at one end. When the shaft 234is inserted in the compressor tube 230, the end of the threaded shaft234 and/or the collet 236 may be exposed beyond the end of thecompressor tube 230 (e.g., as shown in FIG. 5). The button 228 may bedepressed to slide the threaded shaft 234 through the first and secondtubular members 208, 210.

As best seen in FIG. 4, the cord 140 may be inserted into an opening inthe collet 236. The cord 140 may be secured to the collet 236, forexample, with a fastener 238. The fastener 238 may be a threaded setscrew or any other suitable mechanism for securing the cord 140 to theshaft 234. In the alternative, the collet 236 with the cord 140previously connected thereto may be threaded onto the threaded shaft 234to thereby secure the cord 140 to shaft 234.

The instrument 200 is operated by exerting a pull on the cord 140relative to the sheath or tube 230 with the hand lever, as a result, thecalipers or handles 212, 214 are compressed together. The rod or cord140 may be attached to the flexible threaded rod 234 using the collet236. The collet 236 may automatically grab the rod or cord 140 whenpulled into the tube 230. It may be advantageous that both the flexiblethreaded rod 234 and tube 230 are pliable, thereby making it easier forthe surgeon to guide the rod or cord 140 to a fastener 110 within thepleural space.

According to one embodiment, the procedure may follow the followingsequence: (1) the patient may be placed in the lateral decubitusposition with the convexity of the scoliotic curve facing up; (2)monoaxial pedicle screws 110 may be placed across the appropriatevertebral bodies, either through ports or through an open surgicalexposure; (3) the compressor instrument 200 is assembled by pushingcompressor tube 230 into the end and sliding flexible threaded rod 234into the tube 230; (4) the rod (for fusion surgery) or cord 140 (fornon-fusion surgery) is attached to collet 236 and pulled into the tube230; (5) the tube 230 is inserted into the pleural space through eitheran incision or a port placed into an incision, which is placed caudallyto the most caudal fastener 110; (6) the most cranial fastener 110 islocated and the rod or cord 140 is placed into the yoke or head 116 ofthat screw and captured with a counter-torque; and the locking cap 130of the fastener 1120 is tightened on the rod or cord 140; (7) the tube230 is pulled back to expose more of the rod or cord 140, which is thenplaced into the yoke or head 116 of the adjacent (caudal) fastener 1120and captured with the counter-torque; (8) the tube 230 is pushed forwarduntil it abuts the countertorque; the compressor handles 212, 214 aresqueezed until the desired compression force is achieved on the spine;and the locking cap 130 is fully tightened by threading the innerportion 134 of the locking cap 130 onto the cord 140; (9) steps 7 and 8are repeated for the remainder of the screws 110; and (10) in the casewhere a rod has been implanted, the collet 236 is loosened and thecompressor instrument 200 is removed from the pleural space; or in thecase where a cord 140 has been implanted, the cord 140 may be cut withan electrocautery device, scalpel, scissors, or the like; and thecompressor 200 is removed from the pleural space.

Turning now to FIG. 8, an alternative compression instrument 300,similar to instrument 200 will be described. Instrument 300 is similarin function to instrument 200 and like elements will be labeled with thesame reference numbers. In addition to the features of instrument 200,instrument 300 provides a secondary method of applying compression tothe construct. In this embodiment, the first and second tubular members208, 210 may be additionally expanded apart by threads or anothersimilar mechanism. The expansion of this fine-tuning mechanism increasesthe distance between the lock mechanism and the sheath or tube 230,applying force to the flexible rod 234, which holds the rod or cord 140.In particular, a thumb wheel 302 with threads configured to engage thethreads of the threaded shaft 234 may provide finer control of theamount of compression applied to the rod or cord 140. In conjunctionwith the squeeze handles 212, 214, instrument 300 enables two stages ofcompression for both increased force application and finer control ofapplied force. In other words, handles 212, 214 provide for largeamounts of compression and thumb wheel 302 provides for small amounts ofcompression, thereby allowing the surgeon to pinpoint a precise amountof compression on the rod or cord 140.

Turning now to FIG. 9, an alternative compression instrument 400,similar to instrument 200 will be described. Instrument 400 is similarin function to instrument 200 and like elements will be labeled with thesame reference numbers. In instrument 400, the flexible tube 230 hasbeen replaced with a rigid shaft 402. The rigid shaft 402 interfaceswith the force gauge 227 at the proximal end. The rigid shaft 402 has asmooth channel or cannula which guides the rod or cord 140 and theflexible shaft 234 therein. At the distal tip 404 of the shaft 402, thechannel may be curved, for example, to redirect the path of the capturedrod or cord 140, allowing compression to be applied at an angle orperpendicular to the axial force on the construct.

Turning now to FIGS. 10-16, alternative compression instruments 500 areshown. The compressor 500 may function in a manner similar to instrument200, however, instead of squeeze handles 212, 214, the surgeon may holdtwo separate handles 512, 514 (one in each hand) and pulls them apartfrom one another to impart the compressive forces on the rod or cord140. The main handle 512 grasps the compressor tube 230 and includes aratcheting mechanism 516 and a force gauge 527. The other handle 514,may be in the form of a T-handle, for example, and may have a releasebutton 515 so that it can be easily moved to a comfortable position onthe flexible threaded shaft 234. This embodiment may be a good optionfor applying small compression forces to the spine. As an alternative tothe T-handle 514, a knob 524 may be used. The knob 524 may have aninternal thread and works like a nut when threaded onto the flexibleshaft 234. To facilitate quick movement of the knob 524 along thethreaded shaft 234, an off-axis through hole 518 may be drilled throughthe center of the knob 524, for example. When the knob 524 is tilted(canted), for example, as shown in FIGS. 12 and 15, then the internalthreads are disengaged and the knob 524 can be rapidly pushed or pulledalong the flexible shaft 234. For example, the knob 524 may be movedalong shaft 234 until it abuts the main handle 512, for example, asshown in FIG. 16. Once the knob 524 contacts the main handle 512, theknob 524 can be re-aligned to be coaxial with the flexible shaft 234 andturned to apply compressive force to the spine. The inline handle 514 orknob 524 may tension the cord 140 between the final tightened screw andthe most caudal screw. The compressive force, as indicated by the gauge527 may be up to 150N of compressive force (e.g., indicated in 50Nincrements).

The embodiments described herein can provide large compressive,corrective forces and/or small fine-tuned corrective forces to be placedon the spine, for example, in a minimally invasive surgery. The forcesmay be exerted directly on the fasteners as opposed to indirectlyexerting force on a long, flexible instrument attached to the screws.This allows the surgeon to control the force placed on the spine byoffering force feedback to the surgeon in the form of the force gauge.The allows simplified placement of the cord into the yoke or headportion of an adjacent pedicle screw by simply pivoting the instrumentrelative to an already tightened pedicle screw. These systems canfacilitate scoliosis correction and serve as a means for deformitycorrection with or without fusion.

Although the invention has been described in detail and with referenceto specific embodiments, it will be apparent to one skilled in the artthat various changes and modifications can be made without departingfrom the spirit and scope of the invention. Thus, it is intended thatthe invention covers the modifications and variations of this inventionprovided they come within the scope of the appended claims and theirequivalents. It is expressly intended, for example, that all rangesbroadly recited in this document include within their scope all narrowerranges which fall within the broader ranges. It is also intended thatthe components of the various devices disclosed above may be combined ormodified in any suitable configuration.

What is claimed is:
 1. A spinal system comprising: a fastener systemcomprising a fastener, a staple, and a locking cap, the fastener havinga threaded portion and a head portion configured to move relative to thethreaded portion, the staple including a ring configured to surround thethreaded portion of the fastener and a plurality of prongs configured toengage bone; a cord extending from a first end to a second end, the cordconfigured to be retained within the head portion of the fastener withthe locking cap; and an instrument for tensioning the cord, theinstrument including a body having an opening, the opening receiving acompressor tube, the compressor tube receiving a threaded shafttherethrough, and the cord is configured to be affixed to a distal endof the threaded shaft, wherein movement of the threaded shaft, therebyapplies a compressive force to the cord to tension the cord within thefastener system.
 2. The spinal system of claim 1, wherein the instrumentincludes a first portion and a second portion coupled to the firstportion at a pivot point, thereby pivotally connecting the first andsecond portions together.
 3. The spinal system of claim 2, wherein thefirst portion includes a first tubular member and the second portionincludes a second tubular member.
 4. The spinal system of claim 3,wherein in a first position, the first and second tubular members arealigned along a common axis such that the opening is a centrallongitudinal opening extending through the first and second tubularmembers.
 5. The spinal system of claim 4, wherein in a second position,the first and second tubular members are not aligned along the commonaxis and are angled relative to one another.
 6. The spinal system ofclaim 5, wherein the first portion includes a first handle portionextending from the first tubular member and the second portion includesa second handle portion extending from the second tubular member.
 7. Thespinal system of claim 6, wherein distal ends of the first and secondhandle portions are connected with a ratchet.
 8. The spinal system ofclaim 7, wherein the ratchet extends from the distal end of the secondhandle portion at a pivot, and the ratchet engages with a pawl on thefirst handle portion.
 9. The spinal system of claim 8, wherein theratchet includes a plurality of uni-directional teeth.
 10. The spinalsystem of claim 1, wherein the instrument includes a force gauge and aplurality of indicia, and when the force gauge moves, the plurality ofindicia indicate the amount of compressive force provided by theinstrument.
 11. A spinal system comprising: a first fastener systemcomprising a first fastener, a first staple, and a first locking cap,the first fastener having a first threaded portion and a first headportion configured to move relative to the first threaded portion, thefirst staple including a first ring configured to surround the firstthreaded portion of the first fastener and a first plurality of prongsconfigured to engage bone; a second fastener system comprising a secondfastener, a second staple, and a second locking cap, the second fastenerhaving a second threaded portion and a second head portion configured tomove relative to the second threaded portion, the second stapleincluding a second ring configured to surround the second threadedportion of the second fastener and a second plurality of prongsconfigured to engage bone; a cord extending between the first fastenersystem and the second fastener system; and an instrument for tensioningthe cord between the first fastener system and the second fastenersystem, the instrument comprising a first portion having an opening, theopening receiving a compressor tube, the compressor tube capable ofreceiving a shaft therethrough, the shaft capable of coupling to thecord, wherein the instrument applies a compressive force to the cord totension the cord between the first and second fastener systems.
 12. Thespinal system of claim 11, wherein the instrument includes a secondportion coupled to the first portion at a pivot point, thereby pivotallyconnecting the first and second portions together.
 13. The spinal systemof claim 12, wherein the first portion includes a first tubular memberand the second portion includes a second tubular member.
 14. The spinalsystem of claim 13, wherein in a first position, the first and secondtubular members are aligned along a common axis such that a centrallongitudinal opening extends through the first and second tubularmembers.
 15. The spinal system of claim 14, wherein in a secondposition, the first and second tubular members are not aligned along thecommon axis and are angled relative to one another.
 16. The spinalsystem of claim 15, wherein the first portion includes a first handleportion extending from the first tubular member and the second portionincludes a second handle portion extending from the second tubularmember.
 17. The spinal system of claim 16, wherein distal ends of thefirst and second handle portions are connected with a ratchet.
 18. Thespinal system of claim 17, wherein the ratchet extends from the distalend of the second handle portion at a pivot, and the ratchet engageswith a pawl on the first handle portion.
 19. The spinal system of claim18, wherein the ratchet includes a plurality of uni-directional teeth.20. The spinal system of claim 11, wherein the instrument includes aforce gauge and a plurality of indicia, and when the force gauge moves,the plurality of indicia indicate the amount of compressive forceprovided by the instrument.